Product NDC: | 66993-942 |
Proprietary Name: | Mupirocin Calcium |
Non Proprietary Name: | mupirocin calcium |
Active Ingredient(s): | 20 mg/g & nbsp; mupirocin calcium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66993-942 |
Labeler Name: | Prasco Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050746 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20130128 |
Package NDC: | 66993-942-15 |
Package Description: | 1 TUBE in 1 CARTON (66993-942-15) > 15 g in 1 TUBE |
NDC Code | 66993-942-15 |
Proprietary Name | Mupirocin Calcium |
Package Description | 1 TUBE in 1 CARTON (66993-942-15) > 15 g in 1 TUBE |
Product NDC | 66993-942 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | mupirocin calcium |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130128 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Prasco Laboratories |
Substance Name | MUPIROCIN CALCIUM |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |